Presented During:
Thursday, June 27, 2024: 11:30 AM - 12:45 PM
COEX
Room:
Grand Ballroom 104-105
Poster No:
2439
Submission Type:
Abstract Submission
Authors:
Yasuomi Ouchi1,2, Takafumi Sugi1, Etsuji Yoshikawa3
Institutions:
1Hamamatsu University School of Medicine, Hamamatsu, Japan, 2Hamamatsu Medical Photonics Foundation, Hamamatsu, Japan, 3Hamamatsu Photonics KK, Hamamatsu, Japan
First Author:
Yasuomi Ouchi
Hamamatsu University School of Medicine|Hamamatsu Medical Photonics Foundation
Hamamatsu, Japan|Hamamatsu, Japan
Co-Author(s):
Takafumi Sugi
Hamamatsu University School of Medicine
Hamamatsu, Japan
Introduction:
Coughing is known as a defensive reflex that protects the airways from harmful substances. Clinically, the cough reflex may be impaired by stroke While brain activity during cough was previously examined by functional magnetic resonance imaging (fMRI) with model analysis, this method does not capture the actual brain activity during coughing. To obtain accurate measurements of brain activity during coughing, we use an unrestrained positron emission tomography (PET) system with head motion correction to correct for head motion while a whole-brain scan was performed during a coughing task.
Methods:
Twenty-four healthy right-handed men underwent multiple PET scans with [15O]H2O. We have recently developed a PET camera with a free-moving function that enables imaging during head movement by collecting positron signals every 1 second while correcting head movement every 4 milliseconds (Inubushi et al, Neuroimage 2021). Four tasks were performed during the scan: "resting"; "voluntary cough (VC)", which is simply repeated spontaneous coughing; "induced cough (IC)", where participants cough in response to the stimulating stimulus using the cough-inducing method with tartaric acid (CiTA); and "suppressed cough (SC)," in which cough was suppressed in response to CiTA. For CiTA, a 10% solution of L-tartaric acid was used in the IC and SC tasks, and saline was used as a placebo in the resting and VC tasks. We used 60 s of [15O]H2O data reconstructed after the increase in the PET count of the brain. The dose of [15O]H2O injected was 2.5 MBq/kg per scan. During the [15O]H2O experiment, the number of coughs and the intensity of coughing (cough peak flow) were measured. At the end of each scan, the urge to cough during the task was checked on a 10-point scale using the numerical rating scale. We performed whole brain analyses of [15O]H2O PET data with SPM12, applying a fixed-effect analysis with a multi-participant and multi-condition full factorial design, incorporating all scans from all participants into a single general linear model. This study was approved by the Hamamatsu University School of Medicine Ethics Committee.
Results:
Whole brain analyses of motion-corrected data revealed that VC chiefly activated the supplementary motor cortex and the cerebellum extending to pons. In the IC condition, the infratentorial regions, including the pons, medulla oblongata and cerebellar regions, were activated. In the SC condition, significant activation was found in the superior frontal region covering the sensory cortex and the anterior and middle cingulate cortices. Furthermore, CiTA-related tasks (IC and SC) activated the higher sensory regions of the cerebral cortex and associated brain regions. When the urge to cough was taken into account in this analysis, we found that a wider range of cerebral regions including the cerebral cortex and diencephalon play a role in cough control under sensory stimulation.
Conclusions:
Our PET system allows us to image brain activity without head restriction, and this study is the first to depict brain activity during coughing, suggesting that brain activity during simple cough is controlled chiefly by infratentorial areas. Cough control requires incorporating higher sensory areas of the brain to provide top-down control of information coming from the periphery. The current study partly clarified the underlying mechanism of CiTA, which allows clinicians to predict whether it will be effective before attempting it in stroke patients with brain lesions related to cough control.
Novel Imaging Acquisition Methods:
PET 1
Perception, Attention and Motor Behavior:
Perception: Multisensory and Crossmodal 2
Keywords:
Brainstem
Cerebellum
Cerebral Blood Flow
Data analysis
Perception
Positron Emission Tomography (PET)
Other - cough
1|2Indicates the priority used for review
Provide references using author date format
Inubushi, T. et al. (2021), Neural correlates of head restraint: Unsolicited neuronal activation and dopamine release, Neuroimage, vol. 224,117434